Related Experiment Video
Updated: May 21, 2025

06:26
Pulling Membrane Nanotubes from Giant Unilamellar Vesicles
Published on: December 7, 2017
10.9K
On the coupling between membrane bending and stretching in lipid vesicles
Håkan Wennerström1, Emma Sparr1, Joakim Stenhammar1
1Division of Physical Chemistry, Lund University, P.O. Box 124, S-221 00 Lund, Sweden.
Journal of Colloid and Interface Science
|March 18, 2025
Summary
Lipid vesicle formation is energetically costly. Bilayer thinning in small vesicles reduces bending energy, explaining minimum size limits and influencing protein interactions.
Area of Science:
- Biophysics
- Materials Science
- Physical Chemistry
Background:
- Lipid vesicle formation from lamellar phases incurs significant bending energy costs.
- Membrane bending rigidity is inversely related to bilayer thickness.
Purpose of the Study:
- To model the coupling between bending and stretching in lipid bilayers.
- To analyze the impact of this coupling on vesicle bending energy and thermal fluctuations.
- To investigate the implications for vesicle size limitations and protein adsorption.
Main Methods:
- Development of a simple theoretical model for bilayer bending-stretching coupling.
- Analysis of the model's predictions for spherical lipid vesicles.
- Examination of the relationship between bilayer thinning, free energy, and vesicle stability.
Main Results:
- Bilayer thinning becomes significant in small vesicles, reducing bending energy.
- Thermally excited bending modes lead to a substantial decrease in free energy due to thinning.
- A critical thinning point exists, beyond which vesicles become unstable.
Conclusions:
- Bilayer thinning is a key mechanism reducing the energetic cost of small vesicle formation.
- This effect explains the experimentally observed lower limit for vesicle sizes.
- The curvature-dependent thinning may provide a generic mechanism for protein-membrane interactions.
More Related Videos
Related Concept Videos
Mechanisms of Membrane-bending
2.6K
The living membranes are flexible due to their fluid mosaic nature; however, their bending into different shapes is an active process regulated by specific lipids and proteins. The membrane bending can be transient as seen in vesicles or stable for a long time as in microvilli. Cells regulate the size, location, and duration of the membrane curvature.
Membrane bending can happen due to intrinsic changes in lipid composition or extrinsic association with different proteins. The proteins involved...
Membrane bending can happen due to intrinsic changes in lipid composition or extrinsic association with different proteins. The proteins involved...
2.6K
Pinching-off of Coated Vesicles
3.0K
Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
3.0K
SNAREs and Membrane Fusion
9.7K
Once a transport vesicle has recognized its target organelle, the vesicular membrane needs to fuse with the target membrane to unload the cargo. Transmembrane proteins called SNAREs present on organelle membranes and their vesicles, mediate vesicle fusion.
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
9.7K
Membrane Fluidity
10.8K
Membrane fluidity is explained by the fluid mosaic model of the cell membrane, which describes the plasma membrane structure as a mosaic of components—including phospholipids, cholesterol, proteins, and carbohydrates—that gives the membrane a fluid character.
Mosaic nature of the membrane
The mosaic characteristic of the membrane helps the plasma membrane remain fluid. The integral proteins and lipids exist as separate but loosely-attached molecules in the membrane. The membrane is...
Mosaic nature of the membrane
The mosaic characteristic of the membrane helps the plasma membrane remain fluid. The integral proteins and lipids exist as separate but loosely-attached molecules in the membrane. The membrane is...
10.8K
Mechanisms of Membrane Domain Formation
2.9K
Different physical properties of lipids and proteins allow them to localize and form distinct islands or domains in the membrane. Some membrane domains are formed due to protein-protein interactions, whereas others are formed due to the presence of specific lipids such as sphingolipids and sterols—for example, large proteins, such as bacteriorhodopsin, aggregate and create distinct domains.
Another mechanism for membrane domain formation involves membrane proteins interacting with...
Another mechanism for membrane domain formation involves membrane proteins interacting with...
2.9K
Asymmetric Lipid Bilayer
7.1K
Biological membranes show uneven distribution of different types of lipids in the inner and outer layers, resulting in transverse asymmetric membranes. The treatment of the erythrocyte membrane with the enzyme phospholipase confirmed the asymmetric nature of the lipid bilayer. The enzyme hydrolyzes lipids into fatty acids and hydrophilic groups. The phospholipase acts only on the outer layer of the membrane, while the inner layer remains intact. The phospholipase treatment resulted in 80%...
7.1K

